Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-Bromoindole-3-carbaldehyde | HCID 70137 | — |
| Reactant | 6-Hydroxy-3-coumaranone | HCID 235717 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 44554577 | HCID 44554577 | 95% |
Reaction Steps
A solution of 6-hydroxybenzofuran-3(2H)-one (0.50 g, 3.3 mmol) and 5-bromo-1H-indole-3-carboxaldehyde (0.90 g, 4.0 mmol) in ethanol (10 mL) was added with concentrated hydrochloric acid (1.0 mL), and the mixture was stirred at 75° C. for 2 hours. The reaction mixture was cooled to room temperature, and then the solid was collected by filtration, and washed with methanol to obtain (Z)-2-[(5-bromo-1H-indol-3-yl)methylene]-6-hydroxybenzofuran-3(2H)-one (1.1 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09156827B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8de33814ac454e6780cd6775c16a5728 |
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| Source note | uspto-grants-2015_10 |
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